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Controlling Mesenchyme Tissue Remodeling via Spatial Arrangement of Mechanical Constraints
Tissue morphogenetic remodeling plays an important role in tissue repair and homeostasis and is often governed by mechanical stresses. In this study, we integrated an in vitro mesenchymal tissue experimental model with a volumetric contraction-based computational model to investigate how geometrical...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8896258/ https://www.ncbi.nlm.nih.gov/pubmed/35252142 http://dx.doi.org/10.3389/fbioe.2022.833595 |
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author | Winston, Tackla S. Chen, Chao Suddhapas, Kantaphon Tarris, Bearett A. Elattar, Saif Sun, Shiyang Zhang, Teng Ma, Zhen |
author_facet | Winston, Tackla S. Chen, Chao Suddhapas, Kantaphon Tarris, Bearett A. Elattar, Saif Sun, Shiyang Zhang, Teng Ma, Zhen |
author_sort | Winston, Tackla S. |
collection | PubMed |
description | Tissue morphogenetic remodeling plays an important role in tissue repair and homeostasis and is often governed by mechanical stresses. In this study, we integrated an in vitro mesenchymal tissue experimental model with a volumetric contraction-based computational model to investigate how geometrical designs of tissue mechanical constraints affect the tissue remodeling processes. Both experimental data and simulation results verified that the standing posts resisted the bulk contraction of the tissues, leading to tissue thinning around the posts as gap extension and inward remodeling at the edges as tissue compaction. We changed the geometrical designs for the engineered mesenchymal tissues with different shapes of posts arrangements (triangle vs. square), different side lengths (6 mm vs. 8 mm), and insertion of a center post. Both experimental data and simulation results showed similar trends of tissue morphological changes of significant increase of gap extension and deflection compaction with larger tissues. Additionally, insertion of center post changed the mechanical stress distribution within the tissues and stabilized the tissue remodeling. This experimental-computational integrated model can be considered as a promising initiative for future mechanistic understanding of the relationship between mechanical design and tissue remodeling, which could possibly provide design rationale for tissue stability and manufacturing. |
format | Online Article Text |
id | pubmed-8896258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88962582022-03-05 Controlling Mesenchyme Tissue Remodeling via Spatial Arrangement of Mechanical Constraints Winston, Tackla S. Chen, Chao Suddhapas, Kantaphon Tarris, Bearett A. Elattar, Saif Sun, Shiyang Zhang, Teng Ma, Zhen Front Bioeng Biotechnol Bioengineering and Biotechnology Tissue morphogenetic remodeling plays an important role in tissue repair and homeostasis and is often governed by mechanical stresses. In this study, we integrated an in vitro mesenchymal tissue experimental model with a volumetric contraction-based computational model to investigate how geometrical designs of tissue mechanical constraints affect the tissue remodeling processes. Both experimental data and simulation results verified that the standing posts resisted the bulk contraction of the tissues, leading to tissue thinning around the posts as gap extension and inward remodeling at the edges as tissue compaction. We changed the geometrical designs for the engineered mesenchymal tissues with different shapes of posts arrangements (triangle vs. square), different side lengths (6 mm vs. 8 mm), and insertion of a center post. Both experimental data and simulation results showed similar trends of tissue morphological changes of significant increase of gap extension and deflection compaction with larger tissues. Additionally, insertion of center post changed the mechanical stress distribution within the tissues and stabilized the tissue remodeling. This experimental-computational integrated model can be considered as a promising initiative for future mechanistic understanding of the relationship between mechanical design and tissue remodeling, which could possibly provide design rationale for tissue stability and manufacturing. Frontiers Media S.A. 2022-02-18 /pmc/articles/PMC8896258/ /pubmed/35252142 http://dx.doi.org/10.3389/fbioe.2022.833595 Text en Copyright © 2022 Winston, Chen, Suddhapas, Tarris, Elattar, Sun, Zhang and Ma. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Winston, Tackla S. Chen, Chao Suddhapas, Kantaphon Tarris, Bearett A. Elattar, Saif Sun, Shiyang Zhang, Teng Ma, Zhen Controlling Mesenchyme Tissue Remodeling via Spatial Arrangement of Mechanical Constraints |
title | Controlling Mesenchyme Tissue Remodeling via Spatial Arrangement of Mechanical Constraints |
title_full | Controlling Mesenchyme Tissue Remodeling via Spatial Arrangement of Mechanical Constraints |
title_fullStr | Controlling Mesenchyme Tissue Remodeling via Spatial Arrangement of Mechanical Constraints |
title_full_unstemmed | Controlling Mesenchyme Tissue Remodeling via Spatial Arrangement of Mechanical Constraints |
title_short | Controlling Mesenchyme Tissue Remodeling via Spatial Arrangement of Mechanical Constraints |
title_sort | controlling mesenchyme tissue remodeling via spatial arrangement of mechanical constraints |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8896258/ https://www.ncbi.nlm.nih.gov/pubmed/35252142 http://dx.doi.org/10.3389/fbioe.2022.833595 |
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